DE69201359T2 - Kosmetisches Mittel enthaltend eine Mischung aus Metalloxide Nanopigmente und Melaninpigmente. - Google Patents
Kosmetisches Mittel enthaltend eine Mischung aus Metalloxide Nanopigmente und Melaninpigmente.Info
- Publication number
- DE69201359T2 DE69201359T2 DE69201359T DE69201359T DE69201359T2 DE 69201359 T2 DE69201359 T2 DE 69201359T2 DE 69201359 T DE69201359 T DE 69201359T DE 69201359 T DE69201359 T DE 69201359T DE 69201359 T2 DE69201359 T2 DE 69201359T2
- Authority
- DE
- Germany
- Prior art keywords
- cosmetic composition
- composition according
- hydroxy
- group
- melanin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 102
- 239000000049 pigment Substances 0.000 title claims abstract description 57
- 239000002537 cosmetic Substances 0.000 title claims abstract description 41
- 229910044991 metal oxide Inorganic materials 0.000 title claims abstract description 28
- 150000004706 metal oxides Chemical class 0.000 title claims abstract description 28
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 title claims description 91
- 210000004209 hair Anatomy 0.000 claims abstract description 22
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 7
- 239000011701 zinc Substances 0.000 claims abstract description 7
- 229910000420 cerium oxide Inorganic materials 0.000 claims abstract description 6
- 239000010936 titanium Substances 0.000 claims abstract description 6
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 6
- -1 fatty acid salts Chemical class 0.000 claims description 37
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 31
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 27
- 230000003647 oxidation Effects 0.000 claims description 26
- 238000007254 oxidation reaction Methods 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 235000011187 glycerol Nutrition 0.000 claims description 18
- 238000011068 loading method Methods 0.000 claims description 17
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 17
- SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 claims description 16
- 235000012239 silicon dioxide Nutrition 0.000 claims description 16
- 239000000377 silicon dioxide Substances 0.000 claims description 16
- 239000000499 gel Substances 0.000 claims description 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 14
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 14
- 239000004408 titanium dioxide Substances 0.000 claims description 14
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 13
- 239000003755 preservative agent Substances 0.000 claims description 13
- 230000000475 sunscreen effect Effects 0.000 claims description 12
- 239000000516 sunscreening agent Substances 0.000 claims description 12
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 claims description 10
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 10
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 10
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 10
- 239000006210 lotion Substances 0.000 claims description 10
- 239000002304 perfume Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 238000004040 coloring Methods 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 7
- 239000011707 mineral Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 101100294115 Caenorhabditis elegans nhr-4 gene Proteins 0.000 claims description 6
- 238000004061 bleaching Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000006071 cream Substances 0.000 claims description 6
- 230000001590 oxidative effect Effects 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- QGJCWKNNWOVPTJ-UHFFFAOYSA-N 2-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2NC(C)=CC2=C1 QGJCWKNNWOVPTJ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052684 Cerium Inorganic materials 0.000 claims description 5
- 235000021355 Stearic acid Nutrition 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 5
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 5
- 239000002243 precursor Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000008117 stearic acid Substances 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- 235000013871 bee wax Nutrition 0.000 claims description 4
- 239000012166 beeswax Substances 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 4
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- 239000006260 foam Substances 0.000 claims description 4
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 3
- 125000004423 acyloxy group Chemical group 0.000 claims description 3
- 239000000443 aerosol Substances 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 239000004411 aluminium Chemical class 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229940063655 aluminum stearate Drugs 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 238000006872 enzymatic polymerization reaction Methods 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 150000002475 indoles Chemical class 0.000 claims description 3
- 235000013336 milk Nutrition 0.000 claims description 3
- 239000008267 milk Substances 0.000 claims description 3
- 210000004080 milk Anatomy 0.000 claims description 3
- 229920000620 organic polymer Polymers 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- 239000001577 tetrasodium phosphonato phosphate Chemical class 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- 238000011282 treatment Methods 0.000 claims description 3
- PBTPMXPHNHNPPD-UHFFFAOYSA-N (5-methoxy-1h-indol-6-yl) acetate Chemical compound C1=C(OC(C)=O)C(OC)=CC2=C1NC=C2 PBTPMXPHNHNPPD-UHFFFAOYSA-N 0.000 claims description 2
- NTOLUQGMBCPVOZ-UHFFFAOYSA-N (6-acetyloxy-1h-indol-5-yl) acetate Chemical compound C1=C(OC(C)=O)C(OC(=O)C)=CC2=C1NC=C2 NTOLUQGMBCPVOZ-UHFFFAOYSA-N 0.000 claims description 2
- FSYSJTXGNHBKHU-UHFFFAOYSA-N (6-hydroxy-1h-indol-5-yl) acetate Chemical compound C1=C(O)C(OC(=O)C)=CC2=C1NC=C2 FSYSJTXGNHBKHU-UHFFFAOYSA-N 0.000 claims description 2
- 125000000204 (C2-C4) acyl group Chemical group 0.000 claims description 2
- OOOVRUXKQGYTPJ-UHFFFAOYSA-N 1-methylindol-6-ol Chemical compound C1=C(O)C=C2N(C)C=CC2=C1 OOOVRUXKQGYTPJ-UHFFFAOYSA-N 0.000 claims description 2
- ZCBIFHNDZBSCEP-UHFFFAOYSA-N 1H-indol-5-amine Chemical compound NC1=CC=C2NC=CC2=C1 ZCBIFHNDZBSCEP-UHFFFAOYSA-N 0.000 claims description 2
- WTFWZOSMUGZKNZ-UHFFFAOYSA-N 1H-indol-7-amine Chemical compound NC1=CC=CC2=C1NC=C2 WTFWZOSMUGZKNZ-UHFFFAOYSA-N 0.000 claims description 2
- MIMYTSWNVBMNRH-UHFFFAOYSA-N 1h-indol-6-amine Chemical compound NC1=CC=C2C=CNC2=C1 MIMYTSWNVBMNRH-UHFFFAOYSA-N 0.000 claims description 2
- XAWPKHNOFIWWNZ-UHFFFAOYSA-N 1h-indol-6-ol Chemical compound OC1=CC=C2C=CNC2=C1 XAWPKHNOFIWWNZ-UHFFFAOYSA-N 0.000 claims description 2
- ORVPXPKEZLTMNW-UHFFFAOYSA-N 1h-indol-7-ol Chemical compound OC1=CC=CC2=C1NC=C2 ORVPXPKEZLTMNW-UHFFFAOYSA-N 0.000 claims description 2
- KJWHNCIWSFQFCA-UHFFFAOYSA-N 2,3,4,5-tetramethyl-1h-indol-6-amine Chemical compound NC1=C(C)C(C)=C2C(C)=C(C)NC2=C1 KJWHNCIWSFQFCA-UHFFFAOYSA-N 0.000 claims description 2
- UWLICOAZFWOHBB-UHFFFAOYSA-N 2,3,4-trimethyl-1h-indol-6-amine Chemical compound NC1=CC(C)=C2C(C)=C(C)NC2=C1 UWLICOAZFWOHBB-UHFFFAOYSA-N 0.000 claims description 2
- HMOWERPAXOQSFI-UHFFFAOYSA-N 2,3,5-trimethyl-1h-indol-6-amine Chemical compound NC1=C(C)C=C2C(C)=C(C)NC2=C1 HMOWERPAXOQSFI-UHFFFAOYSA-N 0.000 claims description 2
- HMTUVSJLXALWIU-UHFFFAOYSA-N 2,3-dimethyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=C(C)NC2=C1 HMTUVSJLXALWIU-UHFFFAOYSA-N 0.000 claims description 2
- AIMWCCSARFYZCK-UHFFFAOYSA-N 3-methyl-1h-indol-7-ol Chemical compound C1=CC=C2C(C)=CNC2=C1O AIMWCCSARFYZCK-UHFFFAOYSA-N 0.000 claims description 2
- ZUTZCXDHPIACCR-UHFFFAOYSA-N 3-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=CNC2=C1 ZUTZCXDHPIACCR-UHFFFAOYSA-N 0.000 claims description 2
- LUNUNJFSHKSXGQ-UHFFFAOYSA-N 4-Aminoindole Chemical compound NC1=CC=CC2=C1C=CN2 LUNUNJFSHKSXGQ-UHFFFAOYSA-N 0.000 claims description 2
- NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-UHFFFAOYSA-N 0.000 claims description 2
- JEUGWNYIRZKHDS-UHFFFAOYSA-N 5,6-bis(phenylmethoxy)-1h-indole Chemical compound C=1C=CC=CC=1COC1=CC=2C=CNC=2C=C1OCC1=CC=CC=C1 JEUGWNYIRZKHDS-UHFFFAOYSA-N 0.000 claims description 2
- YFTGOBNOJKXZJC-UHFFFAOYSA-N 5,6-dihydroxyindole-2-carboxylic acid Chemical compound OC1=C(O)C=C2NC(C(=O)O)=CC2=C1 YFTGOBNOJKXZJC-UHFFFAOYSA-N 0.000 claims description 2
- QODBZRNBPUPLEZ-UHFFFAOYSA-N 5,6-dimethoxy-1h-indole Chemical compound C1=C(OC)C(OC)=CC2=C1NC=C2 QODBZRNBPUPLEZ-UHFFFAOYSA-N 0.000 claims description 2
- BIMHWDJKNOMNLD-UHFFFAOYSA-N 5-Hydroxyindole-2-carboxylic acid Chemical compound OC1=CC=C2NC(C(=O)O)=CC2=C1 BIMHWDJKNOMNLD-UHFFFAOYSA-N 0.000 claims description 2
- VASQXZIEEJSNHC-UHFFFAOYSA-N 5-ethoxy-1-methylindol-4-ol Chemical compound CCOC1=CC=C2N(C)C=CC2=C1O VASQXZIEEJSNHC-UHFFFAOYSA-N 0.000 claims description 2
- LYZYLCBKDYUUES-UHFFFAOYSA-N 5-ethoxy-1h-indol-4-ol Chemical compound CCOC1=CC=C2NC=CC2=C1O LYZYLCBKDYUUES-UHFFFAOYSA-N 0.000 claims description 2
- LMIQERWZRIFWNZ-UHFFFAOYSA-N 5-hydroxyindole Chemical compound OC1=CC=C2NC=CC2=C1 LMIQERWZRIFWNZ-UHFFFAOYSA-N 0.000 claims description 2
- NUMLTQFTLCZMRX-UHFFFAOYSA-N 5-methoxy-1h-indol-4-ol Chemical compound COC1=CC=C2NC=CC2=C1O NUMLTQFTLCZMRX-UHFFFAOYSA-N 0.000 claims description 2
- RWEBZZKCIMKUTO-UHFFFAOYSA-N 5-methoxy-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC=C2 RWEBZZKCIMKUTO-UHFFFAOYSA-N 0.000 claims description 2
- WEJIMFZPTNVPJQ-UHFFFAOYSA-N 5-methoxy-2,3-dimethyl-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC(C)=C2C WEJIMFZPTNVPJQ-UHFFFAOYSA-N 0.000 claims description 2
- KCZRTDKNQXMPHR-UHFFFAOYSA-N 5-methoxy-2-methyl-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC(C)=C2 KCZRTDKNQXMPHR-UHFFFAOYSA-N 0.000 claims description 2
- HXCHORPNRVSDCD-UHFFFAOYSA-N 5h-[1,3]dioxolo[4,5-f]indole Chemical compound C1=C2OCOC2=CC2=C1NC=C2 HXCHORPNRVSDCD-UHFFFAOYSA-N 0.000 claims description 2
- PFHNYIZEVUEETC-UHFFFAOYSA-N 6-hydroxy-5-methyl-1h-indole-2-carboxylic acid Chemical compound C1=C(O)C(C)=CC2=C1NC(C(O)=O)=C2 PFHNYIZEVUEETC-UHFFFAOYSA-N 0.000 claims description 2
- WZARGPVIAOAKMH-UHFFFAOYSA-N 6-methoxy-1h-indol-5-ol Chemical compound C1=C(O)C(OC)=CC2=C1C=CN2 WZARGPVIAOAKMH-UHFFFAOYSA-N 0.000 claims description 2
- ZOSZXSMIVVPOQH-UHFFFAOYSA-N 6-methoxy-2,3-dimethyl-1h-indol-5-ol Chemical compound C1=C(O)C(OC)=CC2=C1C(C)=C(C)N2 ZOSZXSMIVVPOQH-UHFFFAOYSA-N 0.000 claims description 2
- MVKYMRASKNZUGO-UHFFFAOYSA-N 7-methoxy-1h-indol-6-ol Chemical compound COC1=C(O)C=CC2=C1NC=C2 MVKYMRASKNZUGO-UHFFFAOYSA-N 0.000 claims description 2
- GCMRLOYLVFJGGA-UHFFFAOYSA-N 7-methoxy-2,3-dimethyl-1h-indol-4-ol Chemical compound COC1=CC=C(O)C2=C1NC(C)=C2C GCMRLOYLVFJGGA-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- VXOSJAYSAUDUOR-UHFFFAOYSA-N N-methyl-5,6-dihydroxyindole Chemical compound OC1=C(O)C=C2N(C)C=CC2=C1 VXOSJAYSAUDUOR-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 239000002535 acidifier Substances 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 150000004703 alkoxides Chemical class 0.000 claims description 2
- KMJRBSYFFVNPPK-UHFFFAOYSA-K aluminum;dodecanoate Chemical compound [Al+3].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O KMJRBSYFFVNPPK-UHFFFAOYSA-K 0.000 claims description 2
- 235000001014 amino acid Nutrition 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 230000001680 brushing effect Effects 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- LOEPZYUWYZWRJE-UHFFFAOYSA-N ethyl 5,6-dihydroxy-1h-indole-2-carboxylate Chemical compound OC1=C(O)C=C2NC(C(=O)OCC)=CC2=C1 LOEPZYUWYZWRJE-UHFFFAOYSA-N 0.000 claims description 2
- WANAXLMRGYGCPC-UHFFFAOYSA-N ethyl 5-hydroxy-1h-indole-2-carboxylate Chemical compound OC1=CC=C2NC(C(=O)OCC)=CC2=C1 WANAXLMRGYGCPC-UHFFFAOYSA-N 0.000 claims description 2
- FVMVBNSCNRLYIJ-UHFFFAOYSA-N ethyl 6-hydroxy-1h-indole-2-carboxylate Chemical compound C1=C(O)C=C2NC(C(=O)OCC)=CC2=C1 FVMVBNSCNRLYIJ-UHFFFAOYSA-N 0.000 claims description 2
- 210000004709 eyebrow Anatomy 0.000 claims description 2
- 210000000720 eyelash Anatomy 0.000 claims description 2
- 210000000744 eyelid Anatomy 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000003840 hydrochlorides Chemical class 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- 125000005191 hydroxyalkylamino group Chemical group 0.000 claims description 2
- 229920000592 inorganic polymer Polymers 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- FRVCGRDGKAINSV-UHFFFAOYSA-L iron(2+);octadecanoate Chemical compound [Fe+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O FRVCGRDGKAINSV-UHFFFAOYSA-L 0.000 claims description 2
- 239000000787 lecithin Substances 0.000 claims description 2
- 235000010445 lecithin Nutrition 0.000 claims description 2
- 239000002184 metal Chemical class 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-M methanesulfonate group Chemical class CS(=O)(=O)[O-] AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 claims description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
- 235000011837 pasties Nutrition 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 239000011591 potassium Chemical class 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000003380 propellant Substances 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- 239000002453 shampoo Substances 0.000 claims description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 210000003491 skin Anatomy 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 238000004381 surface treatment Methods 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 229920005613 synthetic organic polymer Polymers 0.000 claims description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical class [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims 2
- NPHFOFOYWYLBTF-UHFFFAOYSA-N 3-methyl-1h-indol-5-ol Chemical compound C1=C(O)C=C2C(C)=CNC2=C1 NPHFOFOYWYLBTF-UHFFFAOYSA-N 0.000 claims 1
- URGMLVWXPXSAKY-UHFFFAOYSA-N 5-methyl-1h-indol-4-ol Chemical compound CC1=CC=C2NC=CC2=C1O URGMLVWXPXSAKY-UHFFFAOYSA-N 0.000 claims 1
- HJUFFOMJRAXIRF-UHFFFAOYSA-N 6-hydroxy-1h-indole-2-carboxylic acid Chemical compound C1=C(O)C=C2NC(C(=O)O)=CC2=C1 HJUFFOMJRAXIRF-UHFFFAOYSA-N 0.000 claims 1
- 230000000887 hydrating effect Effects 0.000 claims 1
- DLINORNFHVEIFE-UHFFFAOYSA-N hydrogen peroxide;zinc Chemical compound [Zn].OO DLINORNFHVEIFE-UHFFFAOYSA-N 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 abstract 1
- 210000002615 epidermis Anatomy 0.000 abstract 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 abstract 1
- 229910001928 zirconium oxide Inorganic materials 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 16
- 239000003921 oil Substances 0.000 description 16
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 14
- 235000019198 oils Nutrition 0.000 description 13
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 12
- 150000003254 radicals Chemical class 0.000 description 9
- 108010076876 Keratins Proteins 0.000 description 8
- 102000011782 Keratins Human genes 0.000 description 8
- RLZLDSDDRORMOV-DBQHITQZSA-M [Na+].Cl.COc1ccc2cc(ccc2c1)[C@H](C)C([O-])=O.CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC Chemical compound [Na+].Cl.COc1ccc2cc(ccc2c1)[C@H](C)C([O-])=O.CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC RLZLDSDDRORMOV-DBQHITQZSA-M 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 8
- 229940099259 vaseline Drugs 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 229960000541 cetyl alcohol Drugs 0.000 description 6
- 235000013980 iron oxide Nutrition 0.000 description 6
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- 230000002335 preservative effect Effects 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 229920002101 Chitin Polymers 0.000 description 5
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 239000004205 dimethyl polysiloxane Substances 0.000 description 5
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
- 229960004418 trolamine Drugs 0.000 description 5
- 229920001661 Chitosan Polymers 0.000 description 4
- 241001562081 Ikeda Species 0.000 description 4
- 239000004166 Lanolin Substances 0.000 description 4
- GEHJBWKLJVFKPS-UHFFFAOYSA-N bromochloroacetic acid Chemical compound OC(=O)C(Cl)Br GEHJBWKLJVFKPS-UHFFFAOYSA-N 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 235000010980 cellulose Nutrition 0.000 description 4
- 229920006037 cross link polymer Polymers 0.000 description 4
- 229940039717 lanolin Drugs 0.000 description 4
- 235000019388 lanolin Nutrition 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 235000014692 zinc oxide Nutrition 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 229940086555 cyclomethicone Drugs 0.000 description 3
- 229940075529 glyceryl stearate Drugs 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004264 Petrolatum Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- NWGKJDSIEKMTRX-BFWOXRRGSA-N [(2r)-2-[(3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)C1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-BFWOXRRGSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 229940072106 hydroxystearate Drugs 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 2
- 239000000391 magnesium silicate Substances 0.000 description 2
- 229910052919 magnesium silicate Inorganic materials 0.000 description 2
- 235000019792 magnesium silicate Nutrition 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229940056211 paraffin Drugs 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 229940066842 petrolatum Drugs 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical group [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- WOAHJDHKFWSLKE-UHFFFAOYSA-N 1,2-benzoquinone Chemical compound O=C1C=CC=CC1=O WOAHJDHKFWSLKE-UHFFFAOYSA-N 0.000 description 1
- 150000004055 1,2-benzoquinones Chemical class 0.000 description 1
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
- 150000004057 1,4-benzoquinones Chemical class 0.000 description 1
- 150000000191 1,4-naphthoquinones Chemical class 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- QHZLMUACJMDIAE-UHFFFAOYSA-N 1-monopalmitoylglycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 description 1
- YPDHDSNSNZOPLI-UHFFFAOYSA-N 2,3-dimethyl-1h-indol-6-amine Chemical compound NC1=CC=C2C(C)=C(C)NC2=C1 YPDHDSNSNZOPLI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- KKAKSARSPPSZFR-UHFFFAOYSA-N 2-[(1-methylindol-6-yl)amino]ethanol Chemical compound C1=C(NCCO)C=C2N(C)C=CC2=C1 KKAKSARSPPSZFR-UHFFFAOYSA-N 0.000 description 1
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 241000238366 Cephalopoda Species 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 102000016942 Elastin Human genes 0.000 description 1
- 108010014258 Elastin Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 108010022355 Fibroins Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 description 1
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- OQILCOQZDHPEAZ-UHFFFAOYSA-N Palmitinsaeure-octylester Natural products CCCCCCCCCCCCCCCC(=O)OCCCCCCCC OQILCOQZDHPEAZ-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000238371 Sepiidae Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940107816 ammonium iodide Drugs 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 229940000635 beta-alanine Drugs 0.000 description 1
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N cystine group Chemical group C([C@@H](C(=O)O)N)SSC[C@@H](C(=O)O)N LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- DLAHAXOYRFRPFQ-UHFFFAOYSA-N dodecyl benzoate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC=CC=C1 DLAHAXOYRFRPFQ-UHFFFAOYSA-N 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- 229920002549 elastin Polymers 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940074052 glyceryl isostearate Drugs 0.000 description 1
- 229940096898 glyceryl palmitate Drugs 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- ASKIVFGGGGIGKH-UHFFFAOYSA-N isostearic acid monoglyceride Natural products CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229940057867 methyl lactate Drugs 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 238000002703 mutagenesis Methods 0.000 description 1
- 231100000350 mutagenesis Toxicity 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical class CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005553 polystyrene-acrylate Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 150000003112 potassium compounds Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 229940029614 triethanolamine stearate Drugs 0.000 description 1
- 229960004441 tyrosine Drugs 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/29—Titanium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/61—Surface treated
- A61K2800/62—Coated
- A61K2800/63—More than one coating
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Nanotechnology (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- Crystallography & Structural Chemistry (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Medical Informatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Inorganic Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9107324A FR2677544B1 (fr) | 1991-06-14 | 1991-06-14 | Composition cosmetique contenant un melange de nanopigments d'oxydes metalliques et de pigments melaniques. |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69201359D1 DE69201359D1 (de) | 1995-03-23 |
DE69201359T2 true DE69201359T2 (de) | 1995-05-24 |
Family
ID=9413875
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69201359T Expired - Fee Related DE69201359T2 (de) | 1991-06-14 | 1992-06-12 | Kosmetisches Mittel enthaltend eine Mischung aus Metalloxide Nanopigmente und Melaninpigmente. |
Country Status (10)
Country | Link |
---|---|
US (1) | US5695747A (fr) |
EP (1) | EP0518773B1 (fr) |
JP (1) | JP3293880B2 (fr) |
AT (1) | ATE118164T1 (fr) |
CA (1) | CA2071276C (fr) |
DE (1) | DE69201359T2 (fr) |
DK (1) | DK0518773T3 (fr) |
ES (1) | ES2068012T3 (fr) |
FR (1) | FR2677544B1 (fr) |
GR (1) | GR3015927T3 (fr) |
Families Citing this family (240)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2680684B1 (fr) * | 1991-08-29 | 1993-11-12 | Oreal | Composition cosmetique filtrante comprenant un nanopigment d'oxyde metallique et un polymere filtre. |
FR2704554B1 (fr) * | 1993-04-27 | 1995-07-13 | Oreal | Procede de preparation d'un pigment melanique de faible granulometrie et son utilisation en cosmetique. |
US5776241A (en) * | 1993-04-27 | 1998-07-07 | L'oreal | Process for the preparation of a melanic pigment of small particle size and its use in cosmetics |
FR2715843B1 (fr) * | 1994-02-09 | 1996-04-12 | Oreal | Compositions cosmétiques antisolaires, procédé de préparation et utilisation. |
FR2716372B1 (fr) * | 1994-02-18 | 1996-04-12 | Oreal | Compositions cosmétiques antisolaires stables, fluides et/ou fluidifiables, procédé de préparation et utilisation. |
FR2720635B1 (fr) | 1994-06-03 | 1996-07-26 | Oreal | Compositions cosmétiques antisolaires et utilisations. |
FR2724318B1 (fr) * | 1994-09-13 | 1997-01-03 | Oreal | Composition cosmetique prevenant ou attenuant la photo-reactivite de manopigments de dioxyde de titane |
ES2117895T3 (es) * | 1995-07-13 | 1998-08-16 | Oreal | Utilizacion de particulas huecas deformables contra el fotoazulado y/o el blanqueo de una composicion cosmetica y/o dermatologica que contiene pigmentos de oxido de titanio. |
DE19530574A1 (de) * | 1995-08-19 | 1997-02-20 | Basf Ag | Titandioxid-Pigmente |
FR2743004B1 (fr) | 1996-01-03 | 1999-10-01 | Oreal | Procede de dispersion par homogeneisation haute pression de charges pulverulentes dans un support constitue d'au moins une phase organique et/ou d'une phase aqueuse, compositions obtenues et utilisations |
FR2744721B1 (fr) | 1996-02-12 | 1999-06-18 | Oreal | Nouveaux derives insolubles de s-triazine, leur procede de preparation, compositions les contenant et leurs utilisations |
BR9602991A (pt) * | 1996-07-05 | 1998-04-28 | Cosmeticos Natural Ind Com | Composições cosméticas hidratantes e protetoras da pele contra as radiações ultravioleta e infravermelha |
FR2751542B1 (fr) * | 1996-07-29 | 1998-09-11 | Oreal | Composition de protection de la peau ou des cheveux contenant des nanopigments et un organopolysiloxane solide elastomere associe a une phase grasse |
FR2757054B1 (fr) * | 1996-12-16 | 1999-01-15 | Oreal | Pigment melanique composite sous forme de particules comprenant un noyau spherique a base de cire, procedes de preparation et utilisations en cosmetique |
AU736810B2 (en) * | 1996-12-18 | 2001-08-02 | Uv Eclipse Pty Ltd | Treatments for protecting animal hair against sunlight damage during growth |
FR2763851B1 (fr) | 1997-05-28 | 1999-07-09 | Oreal | Compositions comprenant un derive de dibenzoylmethane et un polymere polyamine |
FR2763852B1 (fr) | 1997-05-28 | 1999-07-09 | Oreal | Composition comprenant un derive de l'acide cinnamique et un polymere polyamine |
FR2764602B1 (fr) | 1997-06-11 | 1999-07-30 | Oreal | Composition cosmetique comprenant un amide et nouveaux amides |
US6255044B1 (en) * | 1998-01-21 | 2001-07-03 | Eastman Kodak Company | Silver halide elements that produce sharp images without fixing and processes for their use |
JPH11217219A (ja) * | 1998-01-28 | 1999-08-10 | Nonogawa Shoji Kk | 複合化顔料及びこれを含有する化粧料 |
GB9819366D0 (en) * | 1998-09-04 | 1998-10-28 | Unilever Plc | Antiperspirant material and compositions containing it |
CN1173686C (zh) * | 1998-11-02 | 2004-11-03 | Basf公司 | 含有1,3,5-三嗪衍生物和氧化锌的化妆用或药用制剂 |
FR2789579B1 (fr) | 1999-02-12 | 2002-02-01 | Oreal | Compositions cosmetiques pour la photoprotection de la peau et/ou des cheveux contenant un derive de benzotriazole et une bis-resorcinyl triazine |
FR2789601B1 (fr) * | 1999-02-17 | 2001-05-11 | Rhodia Chimie Sa | Sol organique et compose solide a base d'oxyde de cerium et d'un compose amphiphile et procedes de preparation |
US6165450A (en) * | 1999-05-03 | 2000-12-26 | Em Industries, Inc. | Sprayable sunscreen compositions |
FR2795638B1 (fr) | 1999-07-02 | 2003-05-09 | Oreal | Compositions cosmetiques photoprotectrices et utilisations |
GB9917103D0 (en) | 1999-07-22 | 1999-09-22 | Secr Defence | Barrier cream |
US6187824B1 (en) * | 1999-08-25 | 2001-02-13 | Nyacol Nano Technologies, Inc. | Zinc oxide sol and method of making |
FR2798931B1 (fr) | 1999-09-22 | 2001-11-16 | Oreal | Nouveaux composes indoliques, leur utilisation pour la teinture et le maquillage des matieres keratiniques, compositions les contenant et procedes de teinture |
FR2806907B1 (fr) * | 2000-03-31 | 2003-01-24 | Oreal | Composition cosmetique a base de nanoparticules et de composes organiques du silicium solubles dans l'eau |
US6500415B2 (en) | 2000-06-05 | 2002-12-31 | Showa Denko K.K. | Cosmetic composition |
AU6269101A (en) * | 2000-06-05 | 2001-12-17 | Showa Denko Kk | Cosmetic preparation |
FR2811554B1 (fr) | 2000-07-12 | 2002-09-13 | Oreal | Composition comprenant au moins un filtre uv et un sel de flavylium non substitue en position 3 pour la coloration de la peau et utilisations |
FR2811553B1 (fr) | 2000-07-12 | 2002-09-13 | Oreal | Compositions contenant des composes du type sel de flavylium non substitues en position 3 pour la coloration de la peau et une silicone organomodifiee |
DE10060467B4 (de) * | 2000-12-05 | 2007-02-22 | Wella Ag | Pulverförmiges Blondiermittel oder Haarfärbemittel und Verfahren zu dessen Herstellung |
US8080257B2 (en) | 2000-12-12 | 2011-12-20 | L'oreal S.A. | Cosmetic compositions containing at least one hetero polymer and at least one film-forming silicone resin and methods of using |
FR2817739B1 (fr) | 2000-12-12 | 2005-01-07 | Oreal | Composition cosmetique coloree transparente ou translucide |
US6586483B2 (en) | 2001-01-08 | 2003-07-01 | 3M Innovative Properties Company | Foam including surface-modified nanoparticles |
FR2826264B1 (fr) | 2001-06-26 | 2005-03-04 | Oreal | Solubilisation de derives 1,3,5 triazine par des esters n-acyles d'acide amine |
FR2829696B1 (fr) | 2001-09-17 | 2004-02-27 | Oreal | Utilisation de l'acide pantetheine sulfonique et/ou de ses sels en tant qu'agent anti-radicalaire |
EP1302199A3 (fr) | 2001-10-16 | 2004-07-28 | L'oreal | Compositions pour la coloration de la peau proche du bronzage naturel a base d'un pigment du type monascus et utilisations |
KR20030038046A (ko) * | 2001-11-08 | 2003-05-16 | (주)나노플루이드 | 나노크기의 산화아연 입자 및 그를 함유하는 수계 분산체 |
FR2833164B1 (fr) | 2001-12-07 | 2004-07-16 | Oreal | Compositions cosmetiques antisolaires a base d'un melange synergique de filtres et utilisations |
DE10205920A1 (de) | 2002-02-12 | 2003-08-21 | Itn Nanovation Gmbh | Nanoskaliger Rutil, sowie Verfahren zu dessen Herstellung |
US20040016062A1 (en) * | 2002-03-01 | 2004-01-29 | L'oreal | Nondyeing composition containing a precursor and an oxidation reaction catalyst |
DE20207328U1 (de) * | 2002-05-10 | 2002-10-24 | Schwan-Stabilo Cosmetics GmbH & Co., 90562 Heroldsberg | Lipidhaltige Zubereitung |
US20050008598A1 (en) | 2003-07-11 | 2005-01-13 | Shaoxiang Lu | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
US7026410B2 (en) * | 2002-10-17 | 2006-04-11 | Henkel Corporation | Solventless method for preparation of carboxylic polymers |
IL152486A0 (en) | 2002-10-25 | 2003-05-29 | Meir Eini | Alcohol-free cosmetic and pharmaceutical foam carrier |
US7704518B2 (en) | 2003-08-04 | 2010-04-27 | Foamix, Ltd. | Foamable vehicle and pharmaceutical compositions thereof |
US10117812B2 (en) | 2002-10-25 | 2018-11-06 | Foamix Pharmaceuticals Ltd. | Foamable composition combining a polar solvent and a hydrophobic carrier |
US9211259B2 (en) | 2002-11-29 | 2015-12-15 | Foamix Pharmaceuticals Ltd. | Antibiotic kit and composition and uses thereof |
US20080138296A1 (en) | 2002-10-25 | 2008-06-12 | Foamix Ltd. | Foam prepared from nanoemulsions and uses |
MXPA05004278A (es) | 2002-10-25 | 2005-10-05 | Foamix Ltd | Espuma cosmetica y farmaceutica. |
US9668972B2 (en) | 2002-10-25 | 2017-06-06 | Foamix Pharmaceuticals Ltd. | Nonsteroidal immunomodulating kit and composition and uses thereof |
US9265725B2 (en) | 2002-10-25 | 2016-02-23 | Foamix Pharmaceuticals Ltd. | Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof |
US7700076B2 (en) | 2002-10-25 | 2010-04-20 | Foamix, Ltd. | Penetrating pharmaceutical foam |
FR2847812B1 (fr) * | 2002-11-28 | 2006-04-14 | Louis Dubertret | Composition cosmetique comprenant des nanoparticules fluorescentes comme pigments |
US20040120915A1 (en) * | 2002-12-19 | 2004-06-24 | Kaiyuan Yang | Multifunctional compositions for surface applications |
US7125396B2 (en) | 2002-12-30 | 2006-10-24 | Cardinal Health 303, Inc. | Safety catheter system and method |
US7109247B2 (en) * | 2003-05-30 | 2006-09-19 | 3M Innovative Properties Company | Stabilized particle dispersions containing nanoparticles |
US20040242729A1 (en) * | 2003-05-30 | 2004-12-02 | 3M Innovative Properties Company | Stabilized particle dispersions containing surface-modified inorganic nanoparticles |
US7459146B2 (en) * | 2003-05-30 | 2008-12-02 | 3M Innovative Properties Company | Stabilized aerosol dispersions |
US7074396B2 (en) * | 2003-10-22 | 2006-07-11 | Access Business Group International Llc | Composition and method for protecting both natural and artificial hair color from ultraviolet light damage |
FR2861986B1 (fr) * | 2003-11-07 | 2007-12-14 | Oreal | Composition de maquillage comprenant une emulsion |
EP1426033A3 (fr) * | 2004-01-29 | 2004-09-15 | Wella Aktiengesellschaft | Composition de traitement capillaire sous forme d'emulsion contenant des particules solides |
CA2555121A1 (fr) * | 2004-02-04 | 2005-08-25 | Foamix Ltd. | Mousse cosmetique et pharmaceutique comprenant des matieres solides |
CA2556071A1 (fr) | 2004-02-19 | 2005-09-01 | Toray Industries, Inc. | Solutions de nanofibres, emulsions et gels, methode pour leur production, papiers synthetiques a base de nanofibres et methode pour sa production |
ES2633640T3 (es) | 2004-03-22 | 2017-09-22 | L'oreal | Composición cosmética que comprende un elastómero de silicona poliglicerolado |
US7976831B2 (en) | 2004-04-02 | 2011-07-12 | L'oreal S.A. | Method for treating hair fibers |
FR2868305B1 (fr) | 2004-04-02 | 2006-06-30 | Oreal | Procede de traitement capillaire et utilisation dudit procede |
US20060083702A1 (en) * | 2004-04-02 | 2006-04-20 | Thomas Fondin | Hair fiber treating method |
WO2005097054A1 (fr) * | 2004-04-10 | 2005-10-20 | Cotde Inc. | Nouveau complexe de protection contre les rayons uv et son procede de production |
FR2871688B1 (fr) | 2004-06-16 | 2008-05-16 | Oreal | Procede pour favoriser la penetration d'un actif et composition permettant sa mise en oeuvre |
JP2008506662A (ja) * | 2004-07-13 | 2008-03-06 | ロレアル | 親水性金属酸化物ナノ顔料と低分子量のポリアルキレングリコールとを含む水性光保護組成物;その使用 |
FR2873020A1 (fr) * | 2004-07-13 | 2006-01-20 | Oreal | Composition photoprotectrice aqueuse contenant des nanopigments d'oxyde metallique hydrophiles et un polyalkylglycol de faible masse moleculaire; utilisations |
FR2879447B1 (fr) | 2004-12-17 | 2007-01-26 | Oreal | Procede cosmetique de soin de la peau et kit associe |
FR2879445B1 (fr) | 2004-12-20 | 2007-02-23 | Oreal | Produit autobronzant a deux composants, dispositifs multicompartiments, procede de coloration de la peau. |
FR2879456B1 (fr) | 2004-12-20 | 2007-05-04 | Oreal | Composition solaire comprenant au moins un filtre uv lipophile et au moins une hydroxyalkyluree |
FR2880802B1 (fr) | 2005-01-14 | 2008-12-19 | Sederma Soc Par Actions Simpli | Composition cosmetique ou dermopharmaceutique contenant un extrait d'euglene |
FR2883168B1 (fr) | 2005-03-18 | 2008-01-11 | Oreal | Compositions cosmetiques de soin, renforcement et/ou reparation des substrats keratiniques comprenant des polypeptides kap |
JP2008536949A (ja) * | 2005-05-03 | 2008-09-11 | ザ プロクター アンド ギャンブル カンパニー | ケラチン繊維に適用するための離散粒子凝集体及び/又は粒塊を含む組成物 |
FR2885522B1 (fr) * | 2005-05-13 | 2020-01-10 | Sederma | Composition cosmetique ou dermopharmaceutique contenant de la teprenone |
US8440763B2 (en) | 2005-06-09 | 2013-05-14 | L'oreal S.A. | Cosmetic composition comprising silicone particles |
FR2889808B1 (fr) | 2005-08-17 | 2011-07-22 | Oreal | Utilisation de l'acide 8-hexadecene-1,16-dicarboxylique comme agent de soin destine a favoriser la cohesion de la couche cornee |
FR2890310B1 (fr) | 2005-09-06 | 2009-04-03 | Sederma Soc Par Actions Simpli | Utilisation des protoberberines comme agents regulant l'activite de l'unite pilosebacee |
DE102006015753A1 (de) | 2006-04-04 | 2007-10-11 | Goldschmidt Gmbh | Verwendung von Esterquats in Zusammensetzungen als sandabweisende Substanzen |
AU2006342738B2 (en) * | 2006-04-24 | 2012-06-28 | Ntc S.R.L. | Functional nanomaterials with antibacterial and antiviral activity |
FR2900573B1 (fr) | 2006-05-05 | 2014-05-16 | Sederma Sa | Nouvelles compositions cosmetiques renfermant au moins un peptide contenant au moins un cycle aromatique bloque |
JP5043368B2 (ja) * | 2006-06-07 | 2012-10-10 | 花王株式会社 | 毛髪化粧料 |
AU2007269440A1 (en) * | 2006-06-30 | 2008-01-10 | Nucryst Pharmaceuticals Corp. | Metal-containing formulations and methods of use |
FR2902999B1 (fr) | 2006-07-03 | 2012-09-28 | Oreal | Utilisation de derives c-glycoside a titre d'actif prodesquamant |
FR2904549B1 (fr) | 2006-08-03 | 2012-12-14 | Sederma Sa | Composition comprenant de la sarsasapogenine |
US8211224B2 (en) | 2006-11-09 | 2012-07-03 | Sun Chemical Corp. | Multi-colored lustrous pearlescent pigments and process for making |
US8323396B2 (en) | 2006-11-09 | 2012-12-04 | Sun Chemical Corp. | Orange pearlescent pigments |
US8906154B2 (en) | 2006-11-09 | 2014-12-09 | Sun Chemical Corporation | Coating, ink, or article comprising multi-colored lustrous pearlescent pigments |
US7850775B2 (en) * | 2006-11-09 | 2010-12-14 | Sun Chemical Corporation | Multi-colored lustrous pearlescent pigments |
US8349067B2 (en) * | 2006-11-09 | 2013-01-08 | Sun Chemical Corp. | Multi-colored lustrous pearlescent pigments |
US8221536B2 (en) | 2006-11-09 | 2012-07-17 | Sun Chemical Corp. | Cosmetic comprising multi-colored lustrous pearlescent pigments |
US20080260655A1 (en) | 2006-11-14 | 2008-10-23 | Dov Tamarkin | Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses |
FR2909552B1 (fr) | 2006-12-12 | 2009-11-20 | Oreal | Utilisation cosmetique de l'acide anisique pour favoriser la desquamation |
FR2911503B1 (fr) * | 2007-01-19 | 2009-03-13 | Oreal | Composition cosmetique photoprotectrice aqueuse contenant un filtre uv inorganique et un copolymere di-bloc (polystyrene)-bloc-poly(acide acrylique-stat-acrylate d'alkyle en c1-c4) |
US20080219938A1 (en) * | 2007-03-07 | 2008-09-11 | Grune Guerry L | SPF compositions |
US20080299154A1 (en) * | 2007-05-30 | 2008-12-04 | L'oreal Usa Products, Inc. | Cosmetic hair compositions containing metal-oxide layered pigments and methods of use |
DE102007027030A1 (de) | 2007-06-08 | 2008-12-11 | Evonik Goldschmidt Gmbh | Stabile, niedrigviskose kosmetische Zusammensetzungen enthaltend Esterquats und/oder Dialkylquats |
FR2918269B1 (fr) | 2007-07-06 | 2016-11-25 | Oreal | Composition de protection solaire contenant l'association d'un polymere semi-cristallin et de particules de latex creuses. |
US20090014019A1 (en) * | 2007-07-09 | 2009-01-15 | Park Keith K | Humidor |
FR2918563B1 (fr) | 2007-07-12 | 2009-12-04 | Oreal | Composition photoprotectrice fluide aqueuse a base d'un polymere polyamide a terminaison amide tertiaire. |
US8636982B2 (en) | 2007-08-07 | 2014-01-28 | Foamix Ltd. | Wax foamable vehicle and pharmaceutical compositions thereof |
WO2009069006A2 (fr) | 2007-11-30 | 2009-06-04 | Foamix Ltd. | Peroxyde de benzoyle contenant de la mousse |
WO2009072007A2 (fr) | 2007-12-07 | 2009-06-11 | Foamix Ltd. | Porteurs, formulations, procédés pour formuler des agents actifs instables pour application externe et utilisations associées |
ES2619365T3 (es) | 2007-12-28 | 2017-06-26 | Bridgestone Corporation | Método para fabricar polímeros funcionalizados de hidroxiarilo |
US20090185992A1 (en) * | 2008-01-18 | 2009-07-23 | Christelle Conan | Process for producing iron oxide coated pearlescent pigments |
CN102027082B (zh) * | 2008-04-14 | 2013-09-18 | 陶氏康宁公司 | 硼交联的有机基聚硅氧烷的乳液 |
US20110039087A1 (en) * | 2008-04-14 | 2011-02-17 | Severine Cauvin | Emulsions Of Dilatant Organopolysiloxanes |
EP2276796B1 (fr) * | 2008-04-14 | 2012-12-05 | Dow Corning Corporation | Émulsions d'organopolysiloxanes réticulés par du bore et leur utilisation dans des compositions de soins personnelles |
FR2936146B1 (fr) | 2008-09-24 | 2010-10-08 | Oreal | Utilisations de composes dithiolanes pour la photoprotection de la peau ; nouveaux composes dithiolanes ; compositions les contenant. |
US20110223124A1 (en) * | 2008-10-07 | 2011-09-15 | Drovetskaya Tatiana V | Hair care compositions and methods |
FR2939042B1 (fr) | 2008-11-28 | 2010-11-26 | Oreal | PROCEDE DE DEPIGMENTATION DES MATIERES KERATINIQUES A l'AIDE DE COMPOSES DITHIOLANNES. |
FR2939799B1 (fr) | 2008-12-11 | 2011-03-11 | Sederma Sa | Composition cosmetique comprenant des oligoglucuronanes acetyles. |
EP2210887A1 (fr) | 2009-01-14 | 2010-07-28 | Isdin, S.A. | Dérivés de bis-résorcinyl triazine en tant qu'agents de protection contre le rayonnement UV |
FR2941232B1 (fr) | 2009-01-16 | 2014-08-08 | Sederma Sa | Nouveaux peptides, compositions les comprenant et utilisations cosmetiques et dermo-pharmaceutiques. |
WO2010082177A2 (fr) | 2009-01-16 | 2010-07-22 | Sederma | Nouveaux composés, notamment des peptides, compositions comprenant ces derniers et leurs utilisations dans les domaines cosmétique et dermopharmaceutique |
FR2941231B1 (fr) | 2009-01-16 | 2016-04-01 | Sederma Sa | Nouveaux peptides, compositions les comprenant et utilisations cosmetiques et dermo-pharmaceutiques. |
FR2944435B1 (fr) | 2009-04-17 | 2011-05-27 | Sederma Sa | Composition cosmetique comprenant de l'oridonine |
US20120087872A1 (en) | 2009-04-28 | 2012-04-12 | Foamix Ltd. | Foamable Vehicles and Pharmaceutical Compositions Comprising Aprotic Polar Solvents and Uses Thereof |
FR2945939B1 (fr) | 2009-05-26 | 2011-07-15 | Sederma Sa | Utilisation cosmetique du dipeptide tyr-arg pour lutter contre le relachement cutane. |
BRPI1015573B1 (pt) * | 2009-07-01 | 2019-11-12 | Bridgestone Corp | método para fabricação de interpolímero com funcionalidade hidróxi-arila por polimerização iniciada via radical livre |
WO2011013009A2 (fr) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Compositions hydro-alcooliques moussantes non tensioactives, mousses légères, et leurs utilisations |
CA2769677A1 (fr) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Compositions hydro-alcooliques moussantes a base d'agents non tensioactifs non polymeres, mousses legeres, et leurs utilisations |
CN102482495B (zh) | 2009-09-03 | 2014-09-10 | 道康宁公司 | 具有粘液质硅酮液的个人护理组合物 |
US9849142B2 (en) | 2009-10-02 | 2017-12-26 | Foamix Pharmaceuticals Ltd. | Methods for accelerated return of skin integrity and for the treatment of impetigo |
BR112012007473A2 (pt) | 2009-10-02 | 2019-05-07 | Foamix Ltd | composições tópicas de tetraciclina e respectivo método de uso |
CN102666555B (zh) | 2009-11-25 | 2015-06-03 | 道康宁公司 | 挥发性环状硅氧烷 |
CN102933194A (zh) | 2009-12-18 | 2013-02-13 | 欧莱雅公司 | 涉及能够原位缩合的化合物的美容处理方法 |
FR2954118B1 (fr) * | 2009-12-23 | 2012-04-13 | Oreal | Procede pour colorer les fibres keratiniques mettant en oeuvre au moins un derive d'orthodiphenol un oxyde metallique particulier, un agent alcalinisant sous photoirradiation |
FR2960773B1 (fr) | 2010-06-03 | 2015-12-11 | Oreal | Procedes de traitement cosmetique utilisant un revetement a base d'un polymere polyamide-polyether |
US10842728B2 (en) | 2010-08-09 | 2020-11-24 | Allele Biotechnology & Pharmaceuticals, Inc. | Light-absorbing compositions and methods of use |
US9205284B2 (en) | 2010-08-09 | 2015-12-08 | Allele Biotechnology & Pharmaceuticals, Inc. | Light-absorbing compositions and methods of use |
US9737472B2 (en) | 2010-08-09 | 2017-08-22 | Allele Biotechnology & Pharmaceuticals, Inc. | Light-absorbing compositions and methods of use |
US8637600B2 (en) | 2010-08-11 | 2014-01-28 | Bridgestone Corporation | Processing of rubber compositions including siliceous fillers |
US20130155497A1 (en) | 2010-08-25 | 2013-06-20 | Konica Minolta Advanced Layers, Inc. | Film mirror for solar thermal power generation,emthod for producing film mirror for solar thermal power generation, and reflectng device for solar thermal power generation |
WO2012027728A2 (fr) | 2010-08-27 | 2012-03-01 | Sienna Labs, Inc. | Compositions et méthodes de thermomodulation ciblée |
US9572880B2 (en) | 2010-08-27 | 2017-02-21 | Sienna Biopharmaceuticals, Inc. | Ultrasound delivery of nanoparticles |
FR2967056B1 (fr) | 2010-11-05 | 2012-11-09 | Oreal | Composition solaire fluide aqueuse a base d'un polymere superabsorbant et d'un copolymere reticule d'acide methacrylique et d'acrylate d'alkyle en c1-c4. |
FR2968661B1 (fr) | 2010-12-14 | 2016-01-01 | Oreal | Procede de depigmentation des matieres keratiniques a l'aide de composes thiopyridinones |
FR2969149B1 (fr) | 2010-12-16 | 2012-12-28 | Oreal | Procede de depigmentation des matieres keratiniques a l' aide de composes derives de resorcinol |
RU2013130746A (ru) | 2011-01-28 | 2015-01-10 | Моументив Перформенс Матириалз Гмбх | Уф-фотозащитная косметическая композиция |
FR2975295B1 (fr) | 2011-05-20 | 2014-12-26 | Oreal | Composition cosmetique comprenant un polymere superabsorbant et un glucide choisi parmi les oses, les oligosides et les homopolyholosides |
FR2976482B1 (fr) | 2011-06-16 | 2013-07-19 | Oreal | Utilisation d'un compose comprenant au moins une fonction nucleophile pour capturer les composes carbonyles issus de la reaction entre un ou plusieurs composes constituant le sebum et l'ozone |
WO2013010590A1 (fr) | 2011-07-21 | 2013-01-24 | L'oreal | Composition cosmétique et/ou dermatologique contenant un dérivé de mérocyanine qui comprend des groupes polaires spécifiques constitués de fonctionnalités hydroxyle et éther |
FR2982147B1 (fr) | 2011-11-07 | 2014-03-21 | Oreal | Composition a phase huileuse continue contenant au moins un filtre uv organique lipophile et des particules d'aerogel de silice hydrophobes. |
FR2986422B1 (fr) | 2012-02-06 | 2014-02-21 | Oreal | Composition solaire non pulverulente comprenant une phase huileuse polaire et des particules d'aerogel de silice hydrophobes |
FR2991984B1 (fr) | 2012-06-19 | 2014-07-11 | Oreal | Nouveaux derives de resorcinol et leur application cosmetique |
FR2991986B1 (fr) | 2012-06-19 | 2015-02-27 | Oreal | Nouveaux derives de resorcinol et leurs applications cosmetiques |
FR2991985B1 (fr) | 2012-06-19 | 2019-11-08 | L'oreal | Procede de depigmentation des matieres keratiniques a l'aide de nouveaux composes derives de resorcinol |
FR2992858B1 (fr) | 2012-07-04 | 2015-10-30 | Oreal | Composition cosmetique photoprotectrice. |
EP3272388A1 (fr) | 2012-10-11 | 2018-01-24 | Nanocomposix, Inc. | Compositions et procédés de nanoplaques d'argent |
JP6466344B2 (ja) | 2013-01-21 | 2019-02-06 | ロレアル | メロシアニン並びに親油性ベンゾトリアゾールuv遮蔽剤及び/又はビスレゾルシニルトリアジン化合物を含む化粧用又は皮膚用組成物 |
FR3001216B1 (fr) | 2013-01-21 | 2015-02-27 | Oreal | Composition cosmetique ou dermatologique comprenant une merocyanine, une phase huileuse et un mono-alcanol en c1-c4 |
FR3001138B1 (fr) | 2013-01-21 | 2015-06-19 | Oreal | Composition anhydre cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse |
FR3001136B1 (fr) | 2013-01-21 | 2015-06-19 | Oreal | Emulsion cosmetique ou dermatologique comprenant une merocyanine et un systeme emulsionnant contenant un polymere amphiphile comportant au moins un motif acide acrylamido 2-methylpropane sulfonique |
EP2945603B1 (fr) | 2013-01-21 | 2019-03-27 | L'Oréal | Composition cosmétique ou dermatologique comprenant une mérocyanine et un agent anti-uva du type 2-hydroxybenzophénone à substitution amino et/ou un agent anti-uva organique hydrophile |
FR3001135B1 (fr) * | 2013-01-21 | 2015-06-19 | Oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et un filtre uv inorganique insoluble |
JP6509743B2 (ja) | 2013-01-21 | 2019-05-08 | ロレアル | メロシアニン、有機uvb遮蔽剤及び追加の有機uva遮蔽剤を含む化粧用又は皮膚用組成物 |
FR3001133B1 (fr) | 2013-01-21 | 2015-03-20 | Oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un compose amide particulier |
JP6487337B2 (ja) * | 2013-01-21 | 2019-03-20 | ロレアル | メロシアニンと不溶性有機uv遮蔽剤及び/又は不溶性無機uv遮蔽剤とを含む化粧用又は皮膚用組成物 |
FR3001131B1 (fr) | 2013-01-21 | 2015-06-19 | Oreal | Emulsion cosmetique ou dermatologique comprenant une merocyanine et un systeme emulsionnant contenant un tensioactif gemine. |
FR3001128B1 (fr) | 2013-01-21 | 2015-06-19 | Oreal | Emulsion cosmetique ou dermatologique comprenant une merocyanine et un systeme emulsionnant contenant un sel de metal alcalin d'ester d'acide phosphorique et d'alcool gras |
FR3001137B1 (fr) | 2013-01-21 | 2015-02-27 | Oreal | Emulsion eau-dans-huile cosmetique ou dermatologique comprenant une merocyanine et au moins un polymere emulsionnant du type ester d'acide gras et de glycol polyoxyalkylene |
FR3004351B1 (fr) | 2013-04-16 | 2015-03-27 | Sederma Sa | Prevention et traitement des dommages cutanes lies aux infra-rouges |
US9579276B2 (en) | 2013-12-12 | 2017-02-28 | L'oreal | Clear sunscreen composition for application onto wet or dry skin |
JP6340437B2 (ja) | 2014-05-21 | 2018-06-06 | ダウ シリコーンズ コーポレーション | 架橋アミノシロキサンポリマー及び生成方法 |
CN106456507B (zh) | 2014-05-21 | 2019-05-10 | 美国陶氏有机硅公司 | 交联氨基硅氧烷聚合物的乳液 |
CN106795373B (zh) | 2014-07-23 | 2020-06-05 | 美国陶氏有机硅公司 | 有机硅弹性体组合物 |
FR3024037B1 (fr) | 2014-07-25 | 2018-03-02 | Sederma | Ingredient actif cosmetique ou dermatologique comprenant un melange d'acides dicarboxyliques gras insatures, compositions le comprenant et utilisations cosmetiques ou dermatologiques |
WO2016030839A1 (fr) | 2014-08-28 | 2016-03-03 | L'oreal | Composition gel/gel comprenant un filtre uv |
BR112017010702A2 (pt) | 2014-11-24 | 2018-02-14 | Oreal | composição, uso de um filossilicato sintético, uso cosmético de uma composição, processo de tratamento cosmético, processo cosmético |
FR3030227B1 (fr) | 2014-12-17 | 2018-01-26 | L'oreal | Emulsion stabilisees par des particules composites amphiphiles |
EP3233980B1 (fr) | 2014-12-19 | 2020-02-19 | Dow Silicones Corporation | Procédé de préparation de particules fonctionnalisées |
CN107690329B (zh) | 2015-04-08 | 2021-10-08 | 美国陶氏有机硅公司 | 粘液质有机硅乳液 |
FR3037243B1 (fr) | 2015-06-11 | 2018-11-16 | L'oreal | Composition comprenant un filtre uv, un polymere hydrophile reticule anionique, un tensioactif ayant une hlb inferieure ou egale a 5 et un copolymere silicone |
FR3044239B1 (fr) * | 2015-11-30 | 2017-12-22 | Centre Nat Rech Scient | Emulsions anti-uv stabilisees avec de la lignine et des nanoparticules |
FR3045604B1 (fr) | 2015-12-18 | 2018-01-26 | L'oreal | Procede de depigmentation des matieres keratiniques a l'aide de composes thiopyridinones |
FR3046927B1 (fr) | 2016-01-26 | 2018-03-02 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un ether d'isosorbide |
FR3046930B1 (fr) | 2016-01-26 | 2018-03-02 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un polyalkyleneglycol |
FR3046928B1 (fr) | 2016-01-26 | 2019-08-09 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un amide n-substitue |
FR3046929B1 (fr) | 2016-01-26 | 2018-03-02 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un ester d'acide di ou tricarboxylique |
WO2017136809A1 (fr) | 2016-02-04 | 2017-08-10 | The Cleveland Clinic Foundation | Agents actifs de protection solaire à base de polyhydroxy fullerène et compositions |
US20210188883A1 (en) | 2016-04-27 | 2021-06-24 | Dow Silicones Corporation | Hydrophilic silanes |
US10398641B2 (en) | 2016-09-08 | 2019-09-03 | Foamix Pharmaceuticals Ltd. | Compositions and methods for treating rosacea and acne |
BR112019004971B1 (pt) | 2016-09-22 | 2021-12-07 | Colgate-Palmolive Company | Composições de gel hidratante |
FR3060355B1 (fr) | 2016-12-21 | 2020-01-24 | L'oreal | Emulsion eau-dans-huile contenant la baicaline, une base xanthique, une vitamine b3 et un sel de cation metallique multivalent |
FR3060361B1 (fr) | 2016-12-21 | 2018-12-07 | L'oreal | Emulsion eau-dans-huile comprenant un systeme emulsionnant particulier, une argile lipophile, une poudre d’organopolysiloxane elastomerique enrobee d’une resine de silicone |
FR3060997B1 (fr) | 2016-12-23 | 2019-05-31 | L'oreal | Composition comprenant de la baicaline |
FR3068354B1 (fr) | 2017-06-29 | 2020-07-31 | Oreal | Compositions photoprotectrices comprenant un derive dibenzoylmethane, un compose merocyanine et un compose susceptible d'accepter l'energie de niveau excite triplet du compose dibenzoylmethane |
FR3073402B1 (fr) | 2017-11-15 | 2020-05-15 | L'oreal | Composition comprenant de la baicaline et/ou l’un de ses derives et un polymere acrylique particulier |
FR3073408B1 (fr) | 2017-11-15 | 2019-10-11 | L'oreal | Compositions comprenant au moins un polymere acrylique et au moins un filtre organique insoluble |
FR3073400B1 (fr) | 2017-11-15 | 2024-08-09 | Oreal | Emulsion cosmetique contenant un tensioactif gemine et un polymere lipophile |
FR3073409B1 (fr) | 2017-11-15 | 2019-10-11 | L'oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et un polymere acrylique. |
FR3078891B1 (fr) | 2018-03-16 | 2020-12-25 | Centre Nat Rech Scient | Utilisation d’un extrait d’ilex aquifolium pour le traitement des desordres de la pigmentation et pour le blanchiment de la peau |
FR3083097B1 (fr) | 2018-06-28 | 2020-11-27 | Oreal | Composition cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse comprenant au moins un carbonate d’alkyle ou d’alkylene |
FR3083093A1 (fr) | 2018-06-28 | 2020-01-03 | L'oreal | Composition photoprotectrice comprenant des particules de silice colloidale |
FR3090337B1 (fr) | 2018-12-21 | 2021-10-29 | Oreal | Composition photoprotectrice fluide |
FR3090329B1 (fr) | 2018-12-21 | 2020-12-04 | Oreal | Composition comprenant un filtre UV, un polymère hydrophile réticulé anionique, un tensioactif ayant une HLB inférieure ou égale à 5 et un alcane non volatil |
FR3103705B1 (fr) | 2019-11-29 | 2021-12-17 | Oreal | Composition comprenant un filtre UV, un polymère séquencé à groupe acide phosphonique et une huile hydrocarbonée |
FR3103704B1 (fr) | 2019-11-29 | 2022-07-08 | Oreal | Composition comprenant un filtre UV, un polymère éthylénique à groupe acide phosphonique et une huile hydrocarbonée |
FR3117824A1 (fr) | 2020-12-18 | 2022-06-24 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et une phase huileuse comprenant au moins un ester d’acide citrique |
FR3117825A1 (fr) | 2020-12-18 | 2022-06-24 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine, un filtre UV triazine, et un polysaccharide modifié par des chaînes hydrophobes |
FR3119988B1 (fr) | 2021-02-25 | 2023-12-29 | Oreal | Composition aqueuse comprenant un filtre UV organique, un polymère superabsorbant, de la perlite et un alcool gras |
CN113069372A (zh) * | 2021-04-07 | 2021-07-06 | 广州慈康生物科技有限公司 | 一种基于黑色素包覆粒子的防晒组合物及制备方法 |
FR3122578A1 (fr) | 2021-05-07 | 2022-11-11 | L'oreal | Emulsion huile-dans-eau comprenant un mélange particulier de tensioactifs et l’association d’amidon greffé par un polymère acrylique et d’amidon non greffé par un polymère acrylique |
FR3129590A1 (fr) | 2021-11-26 | 2023-06-02 | Capsum | Dispersion macroscopique solaire sans écorce |
EP4447897A1 (fr) | 2021-12-17 | 2024-10-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et une gamma-butyrolactone et/ou un gamma-butyrolactame |
FR3130598A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et du tétra hydroxycinnamate de di-t-butyle pentaérythrityle |
FR3130595A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant au moins une mérocyanine et un hydrotrope |
FR3130599A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et une gamma-butyrolactone et/ou un gamma-butyrolactame |
FR3141059A1 (fr) | 2022-10-20 | 2024-04-26 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et une gamma-butyrolactone et/ou un gamma-butyrolactame |
FR3130597A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et au moins un diol comportant de 4 à 7 atomes de carbone |
FR3130596A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique et/ou dermatologique comprenant au moins une mérocyanine et au moins de l’acide ascorbique et/ou l’un de ses dérivés |
FR3130594A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et du resvératrol et/ou un dérivé de resvératrol |
FR3130593A1 (fr) | 2021-12-17 | 2023-06-23 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et le dipropylène glycol |
FR3131529A1 (fr) | 2021-12-31 | 2023-07-07 | L'oreal | Kit de personnalisation d’une composition cosmétique |
FR3132637A1 (fr) | 2022-02-15 | 2023-08-18 | L'oreal | Composition cosmétique ou dermatologique comprenant une mérocyanine et un complexe polyionique |
FR3133311A1 (fr) | 2022-03-10 | 2023-09-15 | L'oreal | Composition comprenant au moins un copolymere d’amps®, au moins un alkylpolyglucoside, au moins un filtre uv et du myristate d’isopropyle |
WO2023198923A1 (fr) | 2022-04-15 | 2023-10-19 | L'oreal | Émulsion directe comprenant un filtre uv, un polymère acrylique lipophile, un ester d'acide gras d'un polyol et un tensioactif anionique carboxylique |
FR3146591A1 (fr) | 2023-03-16 | 2024-09-20 | L'oreal | Emulsion directe comprenant un filtre UV, un polymère acrylique lipophile, un ester d’acide gras et de polyol et un tensioactif anionique carboxylique, de pH supérieur ou égal à 6 |
FR3134516A1 (fr) | 2022-04-15 | 2023-10-20 | L'oreal | Emulsion directe comprenant un filtre UV, un polymère acrylique lipophile, un ester d’acide gras et de polyol et un dérivé d’acide aminé |
FR3134715A1 (fr) | 2022-04-26 | 2023-10-27 | Capsum | Composition cosmétique solide solaire comprenant au moins une cavité |
FR3136964A1 (fr) | 2022-06-28 | 2023-12-29 | L'oreal | Emulsion avec un dialkyl carbonate, des esters d’huile de coco, une huile volatile hydrocarbonée et un polymère ester d’acide gras et de glycol polyoxyéthyléné |
FR3136965A1 (fr) | 2022-06-28 | 2023-12-29 | L'oreal | Emulsion avec un dialkyl carbonate, des esters d’huile de coco, des alcanes linéaires en C15-C19, une huile volatile hydrocarbonée et un polymère ester d’acide gras et de glycol polyoxyéthyléné |
FR3138306A1 (fr) | 2022-07-26 | 2024-02-02 | L'oreal | Composition comprenant un filtre UV, un polymère superabsorbant et un phospholipide |
FR3141061A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre organique lipophile, un filtre organique hydrophile, des particules sphériques de silice poreuse, des particules sphériques de cellulose, et une poudre d’acide aminé N-acylé |
WO2024083567A1 (fr) | 2022-10-21 | 2024-04-25 | L'oreal | Composition comprenant un filtre organique lipophile, un filtre organique hydrophile, la teneur en poids en phase grasse étant comprise entre 20 et 70 % |
FR3141060A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre UV organique lipophile, un filtre UV organique hydrophile et un polymère gélifiant hydrophile spécifique |
FR3141062A1 (fr) | 2022-10-21 | 2024-04-26 | L'oreal | Composition comprenant un filtre organique lipophile, un filtre organique hydrophile, avec une quantité en poids de phase grasse entre 20 et 70 % et un ratio massique filtres organiques hydrophiles / filtres organiques lipophiles supérieur à 0,3 |
FR3142897A1 (fr) | 2022-12-09 | 2024-06-14 | L'oreal | Composition comprenant un filtre organique hydrodispersible et au moins un complexe polyionique contenant un polysaccharide cationique et un acide non polymérique ayant au moins 3 valeurs de pKa et/ou l’un de ses sels |
FR3143344A1 (fr) | 2022-12-16 | 2024-06-21 | L'oreal | Composition comprenant un filtre UV, un polymère lipophile convenablement sélectionné, et un carraghénane |
FR3143340A1 (fr) | 2022-12-20 | 2024-06-21 | L'oreal | Kit de soin anti-âge pour les matières kératiniques |
FR3146067A1 (fr) | 2023-02-28 | 2024-08-30 | L'oreal | Composition cosmetique a base d'oxyde de zinc et de bisethyhexyloxyphenol methoxyphenyl triazine |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY100306A (en) * | 1985-12-18 | 1990-08-11 | Kao Corp | Anti-suntan cosmetic composition |
LU86347A1 (fr) * | 1986-03-06 | 1987-11-11 | Oreal | Compositions pour la coloration de la peau a base de derives d'indole |
US5256403A (en) * | 1987-01-05 | 1993-10-26 | Gaskin Frances C | Composition and method for protecting the skin from UV-rays |
US4806344A (en) * | 1987-01-05 | 1989-02-21 | Gaskin Frances C | Sun protectant composition and method |
LU86946A1 (fr) * | 1987-07-17 | 1989-03-08 | Oreal | Poudre ultrafine comportant des pigments melaniques,son procede de preparation et son utilisation en cosmetique |
US5028417A (en) * | 1987-07-20 | 1991-07-02 | Johnson & Johnson Consumer Products, Inc. | Sunscreen compositions |
US4806360A (en) * | 1987-10-23 | 1989-02-21 | Advanced Polymer Systems | Synthetic melanin aggregates |
US5093099A (en) * | 1987-11-16 | 1992-03-03 | Kao Corporation | Flaky powder of zinc oxide and its composition for external use |
FR2640956B1 (fr) * | 1988-12-28 | 1991-09-13 | Norsolor Sa | |
LU87429A1 (fr) * | 1989-01-17 | 1990-07-24 | Oreal | Produit a base de particules de polymere comportant des pigments melaniques,son procede de preparation et son utilisation,en particulier en cosmetique |
US5049381A (en) * | 1989-11-22 | 1991-09-17 | Clairol Incorporated | Skin coloring compositions containing indoles and quaternary ammonium salts |
US5037640A (en) * | 1989-11-22 | 1991-08-06 | Clairol Incorporated | Skin coloring and sunscreening compositions containing indoles and M-nitro alkoxybenzenes |
-
1991
- 1991-06-14 FR FR9107324A patent/FR2677544B1/fr not_active Expired - Fee Related
-
1992
- 1992-06-12 DK DK92401627.2T patent/DK0518773T3/da active
- 1992-06-12 AT AT92401627T patent/ATE118164T1/de not_active IP Right Cessation
- 1992-06-12 DE DE69201359T patent/DE69201359T2/de not_active Expired - Fee Related
- 1992-06-12 EP EP92401627A patent/EP0518773B1/fr not_active Expired - Lifetime
- 1992-06-12 JP JP15373692A patent/JP3293880B2/ja not_active Expired - Fee Related
- 1992-06-12 ES ES92401627T patent/ES2068012T3/es not_active Expired - Lifetime
- 1992-06-15 CA CA002071276A patent/CA2071276C/fr not_active Expired - Fee Related
-
1995
- 1995-04-25 GR GR950401048T patent/GR3015927T3/el unknown
- 1995-05-26 US US08/451,982 patent/US5695747A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CA2071276C (fr) | 2006-05-23 |
DE69201359D1 (de) | 1995-03-23 |
EP0518773B1 (fr) | 1995-02-08 |
DK0518773T3 (da) | 1995-07-03 |
GR3015927T3 (en) | 1995-07-31 |
ES2068012T3 (es) | 1995-04-01 |
US5695747A (en) | 1997-12-09 |
JPH05186323A (ja) | 1993-07-27 |
EP0518773A1 (fr) | 1992-12-16 |
FR2677544A1 (fr) | 1992-12-18 |
ATE118164T1 (de) | 1995-02-15 |
CA2071276A1 (fr) | 1992-12-15 |
FR2677544B1 (fr) | 1993-09-24 |
JP3293880B2 (ja) | 2002-06-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69201359T2 (de) | Kosmetisches Mittel enthaltend eine Mischung aus Metalloxide Nanopigmente und Melaninpigmente. | |
DE69200614T2 (de) | Filterndes kosmetisches Mittel enthaltend eine Mischung aus teilweise oder vollständig neutralisierten Benzol 1,4-di(3-Methyliden-10-Kamphosulfonsäure) und Metalloxid-Nanopigmenten. | |
DE69104154T2 (de) | Produkte auf Basis von Melaninpigment enthaltenden plättchenförmigen Partikeln und Verfahren zu ihrer Herstellung. | |
DE69318912T2 (de) | Melanin-Pigmente zusammen mit Tocopherol enthaltende kosmetische Zusammensetzung und Verfahren zum Schutz der Haut, des Haares | |
DE69306176T2 (de) | Mittel auf basis von anorganischen oder organischen partikeln mit einer indolinverbindung | |
DE69305578T2 (de) | Produkt, bazierend auf gefaerbten mineralteilchen, die ein melanin-pigment enthalten, sein herstellungsverfahren und seine verwendung in der kosmetik | |
DE69003258T2 (de) | Produkte auf der Basis von Melaninpigmente enthaltenden Polymerpartikeln, Verfahren zu ihrer Herstellung und ihre Verwendung, insbesondere in der Kosmetik. | |
DE69310522T2 (de) | Kosmetische zusammensetzung, die feste, mit einem amphoteren polymer überzogene teilchen enthält | |
EP0577820B1 (fr) | Composition cosmetique pour le maquillage contenant un pigment transparent d'oxyde de titane et d'oxyde de silicium | |
US5451254A (en) | Fine dispersion of melanin pigments, its preparation and its use in cosmetics | |
EP0685226B1 (fr) | Compositions cosmétiques photoprotectrices contenant des huiles spécifiques et utilisations | |
DE69300943T3 (de) | Indolin-produkte, ihre verfahren zu deren herstellung sowie ihre verwendung in der kosmetik | |
DE69800513T2 (de) | Zusammensetzung, die ein Dibenzoylmethanderivat und ein Polyaminpolymer enthält | |
DE69601023T2 (de) | Kosmetische Sonnenschutzmittel enthaltend TiO2 Nanopigmenten und eine Acylaminosäure | |
US5776241A (en) | Process for the preparation of a melanic pigment of small particle size and its use in cosmetics |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |